lfts Flashcards

1
Q

why order LFTs

A

confirm clinical suspicioun of potential liver injury or disease or to distinguish between hepatocellular injury (hepatic jaundice) and cholestasis (post hepatic or obstructive jaundice

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2
Q

what tests are used to assess liver function

A

ALT, AST, LP, GGT, bilirubin, albumin and prothrombin time

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3
Q

what tests distinguish between hepatocellular damage and cholestasis

A

ALT, AST, ALP, GGT

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4
Q

What are bilirubin, albumin and PT used to assess

A

the livers synthetic function

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5
Q

more than a 10 fold increase in ALT

A

two arrows

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6
Q

two arrows for ALP

A

more than a 3 fold increase

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7
Q

when is ALT found

A

within hepatocytes and enters the blood following hepatocellular injury

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8
Q

when is ALP found

A

in the liver, bile duct and bone tissues - often raised in liver pathology due to increased synthesis in response to cholestasis as a result

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9
Q

what suggests hepatocellular injury

A

a greater than 10 fold increase in ALT and less than 3 fold increase in ALP

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10
Q

what suggests cholestasis

A

a less than 10 fold increase in ALT and more than 3 fold increase in ALP

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11
Q

what is GGT raised suggestive of

A

biliary epithelial damage and bile flow obstruction

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12
Q

raised ALP and GGT

A

cholestasis

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13
Q

lone ALP rise

A

non hepatobiliary pathology

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14
Q

causes of isolated rise in ALP

A

bony metastases or primary bone tumours, vitamin D defiency, recent bone fractures, renal osteodystrophy

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15
Q

causes of isolated bilirubin rise

A

gilberts syndrome, haemolysis

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16
Q

how to check the livers synthetic functions

A

serum bilirubin, serum albumin, prothrombin time, serum blood glucose

17
Q

normal urine and normal stools

A

pre hepatic cause

18
Q

dark urine and normal stools

A

hepatic cause

19
Q

dark urine and pale stools

A

post hepatic cause (obstructive)

20
Q

causes of conjugated hyperbilirubineamia

A

hepatocellular injury and cholestasis

21
Q

causes if unconjugated hyperbiliruvineamia

A

heamolysis, impaired hepatic uptake, impaired conjugation

22
Q

what causes dark urine

A

conjugated bilirubin

23
Q

what causes pale bulky difficuly to flush stool

A

obstructive post hepatic pathology

24
Q

what does albumin do

A

helps bind water, cations, fatty acids and bilirubin and plays a role in oncotic pressure of the blood

25
Q

why can albumin fall

A

liver disease, inflammation, protein losing enteropathies or nephrotic syndrome

26
Q

what is PT

A

the measure of the bloods coagulation tendncy specificlly the extrinsic pathway. In the absence of other decondary causes such as anticoagulant drug use and vit K deficiency an increased PT can indicate liver disease and dysfinction. The liver is responsible for the syntheiss of clotting factors therefore hepatic pathology can impair this process resulting in increased prothrombin time

27
Q

ALT>AST

A

chronic liver disease

28
Q

AST>ALT

A

cirrhosis and acute alcholic hepatitis

29
Q

common causes of acute hepatocellular injury

A

poisoning, infection, liver ischaemia

30
Q

common causes of chronic hepatocellular injury

A

alcoholic fatty liver disease, non alcoholic fatty liver disease, chronic infection, primary biliary cirrhosis